857459

N-Acetyl-L-phenylalanine

ReagentPlus^®, 99%

• Sinónimos: (+)-N-Acetylphenylalanine, (S)-2-Acetamido-3-phenylpropanoic acid
• Fórmula lineal: C₆H₅CH₂CH(NHCOCH₃)CO₂H
• Número de CAS: 2018-61-3
• Peso molecular: 207.23
• Número CE: 217-959-8
• Número MDL: MFCD00063158
• Código UNSPSC: 12352209
• eCl@ss: 32160406
• ID de la sustancia en PubChem: 24888445
• NACRES: NA.22

Propiedades

• Nivel de calidad: 100
• Línea del producto: ReagentPlus^®
• Ensayo: 99%
• Formulario: powder
• actividad óptica: [α]22/D +40.0°, c = 1 in methanol
• idoneidad de la reacción: reaction type: C-H Activation; reaction type: solution phase peptide synthesis; reagent type: ligand; reaction type: Peptide Synthesis
• mp: 171-173 °C (lit.)
• aplicaciones: peptide synthesis
• grupo funcional: amine; carboxylic acid
• cadena SMILES: CC(=O)N[C@@H](Cc1ccccc1)C(O)=O
• InChI: 1S/C11H13NO3/c1-8(13)12-10(11(14)15)7-9-5-3-2-4-6-9/h2-6,10H,7H2,1H3,(H,12,13)(H,14,15)/t10-/m0/s1
• Clave InChI: CBQJSKKFNMDLON-JTQLQIEISA-N

Descripción

Descripción general

N-Acetyl-L-phenylalanine is an acetyl analog of L-phenylalanine. It is widely used as a reactant to synthesize methyl or ethyl esters of N-acetyl-L-phenylalanine, which are employed as versatile building blocks in peptide synthesis.

Aplicación

N-Acetyl-L-phenylalanine can be used as a reactant to synthesize:

• N-acetyl phenylalanine methyl ester by esterification reaction with methanol using Mukaiyama′s reagent.
• Acetylaminocyclohexane propanoic acid by rhodium-catalyzed hydrogenation reaction.

Información legal

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable